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Phenethylcarbamate

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Identification
Molecular formula
C11H15NO2
CAS number
1421-86-5
IUPAC name
ethyl N-(1-phenylethylamino)carbamate
State
State

At room temperature, it is in a solid state.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
291.00
Boiling point (Kelvin)
564.15
General information
Molecular weight
206.26g/mol
Molar mass
206.2560g/mol
Density
1.1550g/cm3
Appearence

The compound appears as a white crystalline solid. It is generally found in powder form and can be considered crystalline due to its ordered molecular structure.

Comment on solubility

Solubility of Ethyl N-(1-phenylethylamino)carbamate

Ethyl N-(1-phenylethylamino)carbamate is a compound that exhibits a notable degree of solubility characteristics, making it interesting for various applications. Understanding its solubility behavior is essential, as it influences factors such as bioavailability and interaction with solvents. Here are some key points regarding its solubility:

  • Solvent Compatibility: Ethyl N-(1-phenylethylamino)carbamate is expected to demonstrate solubility in organic solvents due to its hydrophobic aromatic structure. Common solvents for this compound include:
    • Ethyl acetate
    • Toluene
    • Dimethyl sulfoxide (DMSO)
  • Aqueous Solubility: While less soluble in water, due to its hydrophobic characteristics, some level of solubility may still be observed depending on pH and temperature conditions.
  • Temperature Dependence: Like many organic compounds, solubility may increase with higher temperatures, allowing for larger quantities to dissolve.
  • Impact of pH: The solubility of this compound may be affected by the pH of the solution, particularly due to potential ionization of the amine group, enhancing solubility in slightly acidic or basic environments.

In summary, while ethyl N-(1-phenylethylamino)carbamate is predominantly soluble in organic solvents, its aqueous solubility can vary significantly. Understanding these solubility dynamics is crucial for utilizing this compound in formulations and reactions effectively.

Interesting facts

Interesting Facts about Ethyl N-(1-phenylethylamino)carbamate

Ethyl N-(1-phenylethylamino)carbamate is a fascinating compound that has gained attention within various fields of chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound features a unique structure where a carbamate group is connected to an amino group, which is further substituted by a phenylethyl moiety. This structural configuration plays a significant role in its biological activity.
  • Biological Relevance: Ethyl N-(1-phenylethylamino)carbamate has been studied for its potential applications in pharmacology. It may exhibit properties that are beneficial in medicinal chemistry, particularly in developing new therapeutic agents.
  • Versatile Reactions: As a carbamate derivative, it can participate in a variety of chemical transformations, which makes it a valuable intermediate for synthesizing other complex organic molecules.
  • Catalyst for Innovation: The compound serves as a promising candidate for drug discovery, especially due to its ability to mimic amino acids and influence biological pathways.
  • Research Insights: Recent studies have explored its effects on neurotransmitter systems, hinting at its potential role in modulating mood and cognitive functions, although more research is needed to fully understand these mechanisms.

In conclusion, Ethyl N-(1-phenylethylamino)carbamate not only showcases the complexity of organic synthesis but also highlights the role of carbamate derivatives in the development of medicinal chemistry. As researchers continue to explore this compound, its contributions to science and potential therapeutic uses may unfold further.

Synonyms
Carbenzide
3240-20-8
Carbenzide [INN]
ethyl N-(1-phenylethylamino)carbamate
2V9J52KYM0
Hydrazinecarboxylic acid, 2-(1-phenylethyl)-, ethyl ester
Carbenzida [INN-Spanish]
Carbenzida
Carbenzidum
Carbenzidum [INN-Latin]
Ethyl 3-(alpha-methylbenzyl)carbazate
BRN 0747388
UNII-2V9J52KYM0
Carbencida
Carbenzid
Ethyl-3-(alpha-methylbenzyl)carbazate
Carbamic acid, (alpha-methylbenzylamino)-, ethyl ester
ethyl 2-(1-phenylethyl)hydrazinecarboxylate
SCHEMBL2107475
Carbazic acid, 3-(.alpha.-methylbenzyl)-, ethyl ester
CHEMBL2105955
CARBAZIC ACID, 3-(alpha-METHYLBENZYL)-, ETHYL ESTER
DTXSID80863130
NS00123571
Ethyl 2-(1-phenylethyl)hydrazine-1-carboxylate
ETHYL-3-(.ALPHA.-METHYLBENZYL)CARBAZATE
Q5037845